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Job Details

CRA1 or CRA2

Company: Chiltern
Location: St. Petersburg, Russia
Reference: MM896396Rus
Closing Date: 03 Jan 17
Type: Permanent
Salary (£): On Application
Benefits: excellent

Job Summary:

Due to our continuing success and expansion, we are currently looking for experienced Clinical Research Associates to work with our team in Russia.

Requirements:

Due to our continuing success and expansion, we are currently looking for experienced Clinical Research Associates to work with our team in Russia .
 
CRA/ SCRA is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The work will involve Clinical Monitoring activities for designated projects and to monitor specified sites to ensure quality and integrity of data, compliance with Chiltern International or Sponsor’s SOPs, ICH GCP, and regulatory requirements, ensuring study completion on time and within budget
 

Job Primary Functions:

- Setting up clinical trials in a range of therapeutic areas.
 
-To prepare and conduct all site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and close-out visits according to relevant SOPs


- Feasibility work.
 
- To provide appropriate support for the preparation, submission/notification of local regulatory approval if required for local country requirements

PREFERRED SKILLS:

· A BSc or BA degree in a biomedical or related life science, or nursing qualification
 
· Previous CRA experience within clinical research - minimum 12 months
 
· Good clinical knowledge with an understanding of medical terminology
 
· An understanding of the basics of physiology and pharmacology
 
· Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications
 
· Good oral and written communication, organizational skills and personal presentation. The ability to communicate effectively in English.
 
· Experience working in a team environment under time and resource pressures
 
· Understanding of the principles of ICH GCP and regulatory requirements
 
· Experience of the clinical research process and terminology

 ADDITIONAL INFORMATION:

About Chiltern:

Chiltern is the leading, global mid-sized contract research organization that listens to client needs to deliver customized clinical development solutions. Chiltern’s team of more than 4200  works across 47 countries to provide flexible, specialized services, with core competencies in Biopharma, Medical Device and Diagnostics, Oncology, Clinical Analytics and Source. Visit www.chiltern.com to learn more about responsive solutions that are Designed Around You®.
 

This is a full time PERMANENT position. Positions is office-based ( St Petersburg )  but work will be required away from Chiltern offices, at Sponsor offices, and may require national or international travel. May also involve travel to meetings or attendance at conferences. Overnight stays may be required.
 
For a confidential discussion about this opportunity, please telephone our Internal Recruiter Magdalena Mirowska  To apply, please send your CV to magdalena.mirowska@chiltern.com
 
For more extensive information about Chiltern, please visit our web site at www.chiltern.com
 
PLEASE NOTE: AGENCY OR THIRD PARTY APPLICATIONS WILL NOT BE CONSIDERED. THANK YOU.
 

Apply for this job: CRA1 or CRA2

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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